protein_metabolism
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protein metabolism
Basic overview
- proteins conjugated with ubiquitin are destined for degradation
- dietary amino acids and the amino acids that form from catabolism of protein form an amino acid pool
- the fate of these amino acids may take several routes:
- urinary excretion (although most filtered AA's are reabsorbed)
- formation of body protein (some of which is lost as hair, urinary protein, stools, etc)
- formation of hormones, neurotransmitters
- formation of creatine ⇒ phosphyrylcreatine in muscle ⇒ creatinine ⇒ renal excretion
- metabolism to purines & pyrimidines ⇒ RNA & DNA
- glutamine, glycine, and aspartic acid along with active Vitamin B9/folate are used to make purines (adenine (A) and guanine (G) )
- aspartic acid (aspartate) and glutamine are used to make pyrimidines (Cytosine (C), Thymine (T), Uracil (U) )
- excess pyrimidines ⇒ CO2 + NH3 ⇒ urea
- excess purines ⇒ uric acid
- transamination or amination to other AA's
- oxidative deamination in liver:
- ketogenic AA's (leucine, isoleucine, phenylalanine, tyrosine) ⇒ acetoacetate + NH4+ ⇒ urea
- glucogenic AA's (alanine et al ) ⇒ glucose + NH4+ ⇒ urea
- in addition, sulphur containing AA's (ie. cysteine, methionine) are the source of urinary sulphates
- intestinal cells immediately convert almost 100% of dietary purines into uric acid - they are not re-used!
- hence a high-purine diet directly elevates blood uric acid levels and triggers gout - this is not due to a high amino acid diet
- intestinal cells and the liver break dietary pyrimidines down into highly soluble compounds like beta-alanine and beta-amino-isobutyrate which are are easily converted into Acetyl-CoA and Succinyl-CoA which are fed directly into the citric acid cycle (Krebs cycle) to generate energy
- see dietary_DNA_RNA
protein_metabolism.1786071512.txt.gz · Last modified: 2026/08/07 02:58 by gary1